Nebraska Administrative Code
Topic - HEALTH AND HUMAN SERVICES SYSTEM
Title 181 - SPECIAL HEALTH PROGRAMS
Chapter 2 - SCREENING OF INFANTS FOR INHERITED AND CONGENITAL INFANT OR CHILDHOOD-ON SET DISEASES
Section 181-2-003 - SPECIFICATION OF DISEASES

Universal Citation: 181 NE Admin Rules and Regs ch 2 ยง 003

Current through September 17, 2024

All infants born in the state of Nebraska must be tested for the diseases identified in Neb. Rev. Stat. § 71-519 and the following diseases:

(A) Argininosuccinic Acidemia;

(B) Beta-ketothiolase Deficiency;

(C) Carnitine Uptake Defect;

(D) Citrullinemia;

(E) Congenital Adrenal Hyperplasia;

(F) Cystic Fibrosis;

(G) Glutaric Acidemia type 1;

(H) Homocystinuria;

(I) Isovaleric Acidemia;

(J) Long-chain Hydroxyacyl-CoA Dehydrogenase Deficiency;

(K) Maple Syrup Urine Disease;

(L) Methylmalonic Acidemia (Mutase Deficiency);

(M) Methylmalonic Acidemia (Cbl A and B);

(N) Multiple Carboxylase Deficiency;

(O) Propionic Acidemia;

(P) Severe Combined Immune Deficiencies;

(Q) Tyrosinemia;

(R) Trifunctional Protein Deficiency;

(S) Very Long-chain Acyl-CoA Dehydrogenase Deficiency;

(T) 3-Hydroxy 3-Methyl Glutaric Aciduria; and

(U) 3-Methylcrotonyl-CoA Carboxylase Deficiency.

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